Delfan Maryam, Amadeh Juybari Raheleh, Gorgani-Firuzjaee Sattar, Høiriis Nielsen Jens, Delfan Neda, Laher Ismail, Saeidi Ayoub, Granacher Urs, Zouhal Hassane
Department of Exercise Physiology, Faculty of Sport Sciences, Alzahra University, Tehran, Iran.
Department of Medical Laboratory Sciences, School of Allied Health Medicine, AJA University of Medical Sciences, Tehran, Iran.
Front Cardiovasc Med. 2022 Jun 29;9:927956. doi: 10.3389/fcvm.2022.927956. eCollection 2022.
A role for microRNAs is implicated in several biological and pathological processes. We investigated the effects of high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) on molecular markers of diabetic cardiomyopathy in rats.
Eighteen male Wistar rats (260 ± 10 g; aged 8 weeks) with streptozotocin (STZ)-induced type 1 diabetes mellitus (55 mg/kg, IP) were randomly allocated to three groups: control, MICT, and HIIT. The two different training protocols were performed 5 days each week for 5 weeks. Cardiac performance (end-systolic and end-diastolic dimensions, ejection fraction), the expression of miR-206, HSP60, and markers of apoptosis (cleaved PARP and cytochrome C) were determined at the end of the exercise interventions.
Both exercise interventions (HIIT and MICT) decreased blood glucose levels and improved cardiac performance, with greater changes in the HIIT group ( < 0.001, η: 0.909). While the expressions of miR-206 and apoptotic markers decreased in both training protocols ( < 0.001, η: 0.967), HIIT caused greater reductions in apoptotic markers and produced a 20% greater reduction in miR-206 compared with the MICT protocol ( < 0.001). Furthermore, both training protocols enhanced the expression of HSP60 ( < 0.001, η: 0.976), with a nearly 50% greater increase in the HIIT group compared with MICT.
Our results indicate that both exercise protocols, HIIT and MICT, have the potential to reduce diabetic cardiomyopathy by modifying the expression of miR-206 and its downstream targets of apoptosis. It seems however that HIIT is even more effective than MICT to modulate these molecular markers.
微小RNA在多种生物学和病理过程中发挥作用。我们研究了高强度间歇训练(HIIT)和中等强度持续训练(MICT)对大鼠糖尿病性心肌病分子标志物的影响。
18只雄性Wistar大鼠(260±10 g;8周龄),经链脲佐菌素(STZ)诱导产生1型糖尿病(55 mg/kg,腹腔注射),随机分为三组:对照组、MICT组和HIIT组。两种不同的训练方案每周进行5天,共5周。运动干预结束时测定心脏功能(收缩末期和舒张末期内径、射血分数)、miR-206、HSP60的表达以及凋亡标志物(裂解的PARP和细胞色素C)。
两种运动干预(HIIT和MICT)均降低了血糖水平,改善了心脏功能,HIIT组变化更大(P<0.001,η:0.909)。两种训练方案中miR-206和凋亡标志物的表达均降低(P<0.001,η:0.967),但与MICT方案相比,HIIT导致凋亡标志物的降低幅度更大,miR-206的降低幅度高出20%(P<0.001)。此外,两种训练方案均增强了HSP60的表达(P<0.001,η:0.976),与MICT相比,HIIT组的增加幅度近50%。
我们的结果表明,HIIT和MICT这两种运动方案都有可能通过改变miR-206及其下游凋亡靶点的表达来减轻糖尿病性心肌病。然而,似乎HIIT在调节这些分子标志物方面比MICT更有效。